@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_head {
  this: np:hasAssertion dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_assertion;
    np:hasProvenance dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_provenance;
    np:hasPublicationInfo dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_assertion a np:Assertion .
  
  dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_provenance a np:Provenance .
  
  dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_assertion {
  miriam-gene:80198 a ncit:C16612 .
  
  lld:C0005859 a ncit:C7057 .
  
  dgn-gda:DGNc13e8baa91147fd6bf6686d91fc48de5 sio:SIO_000628 miriam-gene:80198, lld:C0005859;
    a sio:SIO_001121 .
}

dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_provenance {
  dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_assertion dcterms:description
      "[Additionally, we show that depletion of MUS81 or SLX4 reduces the high frequency of SCEs in Bloom's syndrome cells, indicating that MUS81 and SLX4 promote SCE formation, in events that may ultimately drive the chromosome instabilities that underpin early-onset cancers associated with Bloom's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:21399624;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP307906.RAfXABF0j8GNDDAOGzC0HRWmOv7sCQW57KVjzBeg7ATa0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}